Alonso A, Breuer B, Bouterfa H, Doenecke D
German Cancer Research Center, Institute of Experimental Pathology, Heidelberg.
EMBO J. 1988 Oct;7(10):3003-8. doi: 10.1002/j.1460-2075.1988.tb03163.x.
We have isolated and characterized cDNA clones coding for the H1 histone subtype H1(0) in mouse teratocarcinoma cells. The mRNA is 2100 nt long and contains a coding sequence which is highly related to that of the human H1(0) gene. Using this cDNA as a probe, we have shown that, in comparison to undifferentiated F9 cells, differentiated F9 teratocarcinoma cells contain large amounts of H1(0) mRNA. This increase takes place very early during differentiation and does not correlate with changes in the rate of cell division. This indicates that the accumulation of H1(0) mRNA is not the result of reduced proliferation. Most likely on the contrary, the increase in the amount of H1(0) and the resulting effects on the formation of high order chromatin structures are parts of the differentiation program induced in F9 cells.
我们已经从小鼠畸胎瘤细胞中分离并鉴定了编码H1组蛋白亚型H1(0)的cDNA克隆。该mRNA长2100个核苷酸,包含一个与人类H1(0)基因编码序列高度相关的编码序列。用这个cDNA作为探针,我们发现,与未分化的F9细胞相比,分化的F9畸胎瘤细胞含有大量的H1(0) mRNA。这种增加在分化过程中很早就发生了,并且与细胞分裂速率的变化无关。这表明H1(0) mRNA的积累不是增殖减少的结果。相反,最有可能的是,H1(0)数量的增加以及由此对高阶染色质结构形成的影响是F9细胞中诱导的分化程序的一部分。